EMG abnormality
Symptom Information:
Symptom ID: | HPO:0003457 | ||||||||||||||||
Synonyms: |
|
||||||||||||||||
Quality: | |||||||||||||||||
Cross references: |
|
||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) EMG abnormality(HPO:0003457) MedDRA: Investigations(MedDRA:10022891) Neurological, special senses and psychiatric investigations(MedDRA:10029295) Neurologic diagnostic procedures(MedDRA:10029285) EMG abnormality(HPO:0003457) |
||||||||||||||||
Database Frequency: | 78 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Adrenomyodystrophy | (Orphanet:977) |
Adult polyglucosan body disease | (Orphanet:206583) |
Antisynthetase syndrome | (Orphanet:81) |
Apolipoprotein A-I deficiency | (Orphanet:425) |
Arthrogryposis due to muscular dystrophy | (Orphanet:1155) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Bethlem myopathy | (Orphanet:610) |
Centronuclear myopathy | (Orphanet:595) |
Cervical hypertrichosis - peripheral neuropathy | (Orphanet:2218) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Choreoacanthocytosis | (Orphanet:2388) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Dermatomyositis | (Orphanet:221) |
Duchenne and Becker muscular dystrophy | (Orphanet:262) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Familial dysautonomia | (Orphanet:1764) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Gemignani syndrome | (Orphanet:2074) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Gyrate atrophy of choroid and retina | (Orphanet:414) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Hypomyelination neuropathy - arthrogryposis | (Orphanet:2680) |
Inclusion body myositis | (Orphanet:611) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile dermatomyositis | (Orphanet:93672) |
Kearns-Sayre syndrome | (Orphanet:480) |
Krabbe disease | (Orphanet:487) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
Macrophagic myofasciitis | (Orphanet:592) |
Marden-Walker syndrome | (Orphanet:2461) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial myopathy - lactic acidosis - deafness | (Orphanet:2597) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Monomelic amyotrophy | (Orphanet:65684) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Muscle-eye-brain disease | (Orphanet:588) |
Muscular dystrophy - white matter spongiosis | (Orphanet:1877) |
Myhre syndrome | (Orphanet:2588) |
Myoclonus - cerebellar ataxia - deafness | (Orphanet:2589) |
Myotonia fluctuans | (Orphanet:99734) |
Myotonia permanens | (Orphanet:99735) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurogenic thoracic outlet syndrome | (Orphanet:100073) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
Neutral lipid storage disease | (Orphanet:165) |
O'Sullivan-McLeod syndrome | (Orphanet:99965) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
Polymyositis | (Orphanet:732) |
Polyneuropathy - intellectual deficit - acromicria - premature menopause | (Orphanet:2928) |
Potassium-aggravated myotonia | (Orphanet:612) |
Primary orthostatic tremor | (Orphanet:238606) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Proximal spinal muscular atrophy type 2 | (Orphanet:83418) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
RIPPLING MUSCLE DISEASE | (OMIM:606072) |
Rippling muscle disease | (Orphanet:97238) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Spastic ataxia - corneal dystrophy | (Orphanet:2572) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Steinert myotonic dystrophy | (Orphanet:273) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Thomsen and Becker disease | (Orphanet:614) |
Thoracic outlet syndrome | (Orphanet:97330) |
Usher syndrome | (Orphanet:886) |
X-linked centronuclear myopathy | (Orphanet:596) |